Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 5
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10773989
ADIPOR2
0.925 0.160 12 1747816 intron variant T/C snv 0.41 5
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs10929251
UGT1A10 ; UGT1A8
1.000 0.080 2 233637583 intron variant A/G snv 0.13 5
rs113686495
CASP8
0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 4
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs17864678
UGT1A10 ; UGT1A8
1.000 0.080 2 233635964 intron variant T/A snv 5.6E-03 5
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28